单克隆抗体
表位
糖蛋白
病毒学
线性表位
抗体
化学
分子生物学
表位定位
生物
主管(地质)
细胞培养
作者
Qianran Wang,Hao Li,Fanchong Jian,Aoxiang Han,Yuanni Liu,Jingyi Liu,Yuanling Yu,Jing Wang,Lingling Yu,Yanxia Wang,Haiyan Sun,Miaomiao Ma,Fei Shao,LiuLuan Zhu,Wei Liu,Yunlong Cao
出处
期刊:Cell Reports
[Cell Press]
日期:2026-04-01
卷期号:45 (4): 117248-117248
标识
DOI:10.1016/j.celrep.2026.117248
摘要
Severe fever with thrombocytopenia syndrome virus (SFTSV) is a lethal bunyavirus lacking approved countermeasures. From SFTS survivors, we isolate 84 human monoclonal antibodies (mAbs) against the viral glycoproteins Gn and Gc. Gn-specific mAbs demonstrate superior neutralization breadth and potency compared to the restricted neutralizing activity observed with Gc. Using a high-throughput yeast display deep mutational scanning (DMS) platform, we classify Gn-head mAbs into eight epitope groups, among which four groups (IA, ID, IIIA, and IIIB) confer neutralization. Notably, mAbs BD70-4003 (group IA) and BD70-4017 (group IIIA) exhibit broad neutralization and provide 100% protection in a lethal mouse model. Cryo-electron microscopy (cryo-EM) structural analysis of these mAbs in complex with the Gn head reveals their binding interfaces, directly validating the epitope residues identified by DMS. Our study delineates the antigenic landscape of SFTSV Gn, identifies potent therapeutic candidates, and establishes DMS coupled with structural validation as a powerful framework for antibody discovery against bunyaviruses.
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